* Minimum 1 year of experience in a chemical/pharmaceutical/medical device manufacturing environment
* Knowledgeable in Good Manufacturing Practices (GMP)
* Proficient in MS Office applications
* Excellent oral and communication skills
* Good team player who can work efficiently with minimal supervision.
* Quality Control experience in a lab setting would be an advantage
* Third-level qualification in Quality/ Engineering, Materials/Science/Mechanical, or Instrumentation would be beneficial
Responsibilities:
* Carry out any process steps required for the manufacture and packing of high-quality products (Storing, retrieving, mixing, and monitoring chemicals used in the production process).
* Adherence to Quality system procedures and all associated manufacturing documentation, which is provided to employees in order to assist them in the manufacture and shipment of high-quality products.
* Troubleshooting issues with production equipment and processes.
* Recording information, such as ingredients, weights, temperature, and in-process inspection, and input into the database.
* Working with other team members to complete the production process.
* Preparing QMS documents that are related production process, such as SOP and Validation documents.
* Responsible for the completion of training in relation to the manufacture and shipment of the product.
* Ensure that a high standard of GMP and housekeeping is maintained in all manufacturing areas.
* Adherence to all Environmental, Health, and Safety requirements in accordance with company Policies.
* Other tasks related may be assigned by the immediate superior from time to time.
Seniority level
* Seniority level
Entry level
Employment type
* Employment type
Full-time
Job function
* Job function
Production
* Industries
Medical Equipment Manufacturing
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